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Thionobencarb

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Identification
Molecular formula
C12H12NO4PS2
CAS number
28249-77-6
IUPAC name
2-(dimethoxyphosphinothioylsulfanylmethyl)isoindoline-1,3-dione
State
State

Thionobencarb is a solid at room temperature, typically in crystalline form.

Melting point (Celsius)
85.50
Melting point (Kelvin)
358.65
Boiling point (Celsius)
441.20
Boiling point (Kelvin)
714.35
General information
Molecular weight
329.34g/mol
Molar mass
329.3380g/mol
Density
1.3500g/cm3
Appearence

Thionobencarb appears as a colorless to light yellow crystalline solid.

Comment on solubility

Solubility of 2-(dimethoxyphosphinothioylsulfanylmethyl)isoindoline-1,3-dione

The solubility of the compound 2-(dimethoxyphosphinothioylsulfanylmethyl)isoindoline-1,3-dione is an intriguing topic, as it can significantly influence its applications in various fields. Understanding its solubility characteristics is vital for formulating effective solutions. Here are some key points regarding the solubility:

  • Polarity: The compound contains both polar and non-polar functional groups, which can affect its solubility in different solvents.
  • Solvent Type: Likely more soluble in polar solvents such as dimethyl sulfoxide (DMSO) or water due to the presence of polar groups.
  • Temperature Influence: Elevating the temperature can enhance solubility, particularly in organic solvents.
  • pH Consideration: The solubility may vary with the pH of the medium, as ionization of the functional groups could play a key role.

It is advisable to perform solubility tests in a controlled laboratory environment to accurately determine the solubility limits and behavior of this compound. Ultimately, these solubility properties will dictate its practical use in synthesis and application, making this an essential topic of study.

Interesting facts

Interesting Facts about 2-(Dimethoxyphosphinothioylsulfanylmethyl)isoindoline-1,3-dione

This intriguing compound is a member of the isoindoline family, which is characterized by its unique bicyclic structure. Isoindolines, like this one, are notable for their various applications in organic synthesis and medicinal chemistry. Here are some fascinating aspects of this particular compound:

  • Versatile Reactivity: The presence of the dimethoxyphosphinothioyl group enhances its reactivity, making it a valuable intermediate for synthesizing other complex molecules.
  • Biological Activity: Compounds featuring isoindoline structures often exhibit significant biological activities, including potential anticancer and antimicrobial properties, making them of great interest in pharmaceutical research.
  • Complex Synthesis: The synthesis of this compound can be quite complex and may involve multiple synthetic steps, often requiring a high level of expertise in organic chemistry.
  • Applications in Agriculture: This compound may also find applications in agriculture as a potential pesticide or herbicide, contributing to the development of safer and more effective crop protection methods.
  • Analytical Techniques: Researchers often employ advanced analytical techniques such as NMR, MS, and IR spectroscopy to fully characterize compounds like this, shedding light on their structure and properties.

Exploring compounds such as 2-(dimethoxyphosphinothioylsulfanylmethyl)isoindoline-1,3-dione allows chemists to not only understand the intricacies of molecular design but also to explore new frontiers in drug discovery and materials science.

As they say in chemistry, "The best way to predict the future is to invent it!" This compound's unique structure and properties could pave the way for significant advancements in various scientific fields.

Synonyms
Phosmet
Fosmet
732-11-6
Decemthion
Phthalophos
Imidathion
Percolate
Ftalophos
Kemolate
Safidon
Simidan
Smidan
Decemthion P-6
PMP (Pesticide)
Phtalofos
Prolate E
Stauffer R 1504
Imidan WP
Prolate 5 Dust
Decemtion P-6
Imidan 5 Dust
O,O-Dimethyl S-phthalimidomethyl phosphorodithioate
Prolate 8-OS
O,O-Dimethyl phthalimidomethyl phosphorodithioate
Caswell No. 543
O,O-Dimethyl S-(phthalimidomethyl) dithiophosphate
CCRIS 5295
ENT 25,705
HSDB 1734
Phthalimido O,O-dimethyl phosphorodithioate
EINECS 211-987-4
UNII-VN04LI540Y
R 1504
EPA Pesticide Chemical Code 059201
Phthalimidomethyl O,O-dimethyl phosphorodithioate
(O,O-Dimethyl-phthalimidiomethyl-dithiophosphate)
BRN 0264869
VN04LI540Y
DTXSID5024261
CHEBI:38786
O,O-Dimethyl S-(N-phthalimidomethyl)dithiophosphate
O,O-Dimethyl S-(phthalimidomethyl)phosphorodithioate
AI3-25705
R-1504
N-(Dimethoxyphosphinothioylthiomethyl)phthalimide
O,O-Dimethyl S-phthalimidomethyl phosphorothionate
O,O-Dimethyl S-(phthalimididomethyl)phosphorodithioate
Phthalimide, N-(mercaptomethyl)-, S-ester with O,O-dimethyl phosphorodithioate
Phosphorodithioic acid, O,O-dimethyl ester, S-ester with N-(mercaptomethyl)phthalimide
Phosphorodithioic acid, S-((1,3-dihydro-1,3-dioxo-isoindol-2-yl)methyl) O,O-dimethyl ester
S-((1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate
DTXCID004261
N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl phosphorodithioate)
O,O-Dimethyl phosphorodithioate S-ester with N-(mercaptomethyl)phthalimide
S-((1,3-Dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate
S-[(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] o,o-dimethyl dithiophosphate
Phosphorodithioic acid O,O-dimethyl ester S-ester with N-(mercaptomethyl) phthalimide
Phosphorodithioic acid, S-((1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethyl ester
S-((1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl) O,O-dimethy phosphorodithioate
S-((1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl)phosphorodithioic acid O,O-dimethyl ester
PHOSMET (MART.)
PHOSMET [MART.]
Phosphorodithioic acid, S-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl] O,O-dimethyl ester
S-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] O,O-dimethyl phosphorodithioate
N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl) phosphorodithioate
N-(MERCAPTOMETHYL) PHTHALIMIDE S-(O,O-DIMETHYL PHOSPHORODITHIOATE)
Del-Phos
S-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl) O,O-dimethyl dithiophosphate
S-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl) O,O-dimethyl phosphorodithioate
Prolate I-E
DECEMTHIO
DECEMTION
ORBISECT
ORDATOX
PORECT
DECEMTHION EK 20
STARBAR GX 118
N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl phosphorothionate)
ENT 25705
USEPA/OPP Pesticide Code: 59201
O,O-Dimethyl 5-(phthalimidomethyl)dithiophosphate
o,o-dimethyl s-(n-phthalimidomethyl) dithiophosphate
(O,O-DIMETHYL-PHTHALIMIDIOMETHYLDITHIOPHOSPHATE)
S-PHTHALIMIDOMETHYL O,O-DIMETHYL PHOSPHORODITHIOATE
N-(mercaptomethyl)phthalamide S-(O,O-dimethyl phosphorodithioate)
O,O-Dimethyl phosphorodithioate S-ester with N-(mercaptomethyl) phthalimide
PHOSPHORODITHIOIC ACID, O,O-DIMETHYL S-PHTHALIMIDOMETHYL ESTER
211-987-4
appa
Prolate
IMIDAN
Phosmet [BAN]
phthalimidomethyl-o,o-dimethyl phosphorodithioate
2-(dimethoxyphosphinothioylsulfanylmethyl)isoindole-1,3-dione
SMR000054364
MLS000104429
MLS001074294
Phosmet (BAN)
NCGC00080392-01
5104-30-3
CAS-732-11-6
Phosmet-d6 100 Amicrog/mL in Acetone
Phosmet [BSI:ISO]
SR-01000195222
Phosmet [BAN:BSI:ISO]
imidan/phosmet
Poron (TN)
Del-Phos (TN)
PHOSMET [HSDB]
PHOSMET [ISO]
PHOSMET [MI]
Opera_ID_1806
CBMicro_004801
SCHEMBL3620
Oprea1_616683
PHOSMET [GREEN BOOK]
cid_12901
CHEMBL1481873
BDBM79427
LMNZTLDVJIUSHT-UHFFFAOYSA-
HMS2230D06
HMS3370L13
SMSF0003235
Tox21_110993
Tox21_202316
Tox21_300093
Phosmet 10 microg/mL in Cyclohexane
Phosmet 1000 microg/mL in Acetone
STK097158
AKOS001603761
Phosmet 100 microg/mL in Cyclohexane
Tox21_110993_1
CB06771
DB11448
Phosmet 100 microg/mL in Acetonitrile
NCGC00080392-02
NCGC00080392-03
NCGC00080392-04
NCGC00080392-05
NCGC00254165-01
NCGC00259865-01
BIM-0004802.P001
DB-055733
Phosmet, PESTANAL(R), analytical standard
NS00000517
C18756
D08372
O,O-Dimethyl S-(phthalimidomethyl)dithiophosphate
Q421379
O,O-dimethyl S-phthalimido methyl phosphorodithioate
SR-01000195222-1
SR-01000195222-4
2-[(dimethoxyphosphinothioylthio)methyl]isoindole-1,3-dione
2-[(dimethoxythiophosphorylthio)methyl]isoindoline-1,3-quinone
S-[(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] O,O-dimethyl dithiophosphate #
InChI=1/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3